FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Lenses, Soft Contact, Extended Wear
PMA: N17679
·
Supplement: S035
·
Decision Apr 29, 2011
Classifications
1
FEI Numbers
56
Registration Numbers
56
Basic Information
- Device Name
- Lenses, Soft Contact, Extended Wear
- Trade Name
- TETRAFILCON A
- PMA Number
- N17679
- Supplement Number
- S035
- Device Class
- FDA Class 3
- Product Code
- LPM
- Generic Name
- Lenses, soft contact, extended wear
- Regulation Number
- 886.5925
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- April 29, 2011
- Date Received
- March 24, 2011
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
CHANGES IN CRITERIA FOR ACCEPTANCE FOR WATER CONTENT FROM 5% TO 2%; AND REVISION TO MAXIMUM SPECIFICATIONS OF LENS MATERIAL COMPONENTS AND THE SPECIFICATION FOR WATER CONTENT.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LPM | Lenses, Soft Contact, Extended Wear | FDA class 3 | Ophthalmic |